42599-17-7 Usage
Description
Trans-1-iodo-1-octene is an organic compound with the molecular formula C8H15I, belonging to the class of alkenes characterized by the presence of a carbon-carbon double bond. trans-1-Iodo-1-octene features a trans configuration, where the iodine atom and the alkene functional group are positioned on opposite sides of the double bond.
Uses
Used in Organic Synthesis:
Trans-1-iodo-1-octene is utilized as a reagent in various chemical reactions due to the iodine atom's propensity to undergo substitution reactions, making it a valuable component in organic synthesis processes.
Used in Pharmaceutical Production:
trans-1-Iodo-1-octene serves as a precursor in the production of pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Agrochemical Manufacturing:
Trans-1-iodo-1-octene is also employed in the manufacturing of agrochemicals, playing a role in the creation of products designed to enhance crop protection and yield.
Used in Dye and Perfume Industries:
trans-1-Iodo-1-octene finds applications in the production of dyes and perfumes, where its unique chemical properties contribute to the development of novel colorants and fragrances.
Used in Materials Science:
Trans-1-iodo-1-octene is used as a precursor for the synthesis of polymers and other advanced materials, showcasing its versatility in the field of materials science and contributing to the development of innovative material technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 42599-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,9 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42599-17:
(7*4)+(6*2)+(5*5)+(4*9)+(3*9)+(2*1)+(1*7)=137
137 % 10 = 7
So 42599-17-7 is a valid CAS Registry Number.
42599-17-7Relevant articles and documents
Vinylic Organoboranes. 9. A General Stereospecific Synthesis of (Z)- and (E)-Disubstituted Alkenes via Organoboranes
Brown, Herbert C.,Basavaiah, Deevi,Kulkarni, Surendra U.,Bhat, Narayan G.,Prasad, J. V. N. Vara
, p. 239 - 246 (2007/10/02)
A general and stereospecific synthesis of (Z)-disubstituted alkenes using mono- and dihaloboranes is presented.The hydridation of dialkylhaloboranes in the presence of 1-alkynes provides the corresponding dialkylvinylboranes (1), representing the first general synthesis of such derivatives.Treatment with iodine in the presence of sodium methoxide induces the migration of one of the alkyl groups from boron to the adjacent carbon, followed by a rapid deiodoboronation to afford (Z)-disubstituted alkenes (2) in high yields.Similarly, the hydroboration of 1-alkynes with alkyl bromoboranes (R1BHBr*SMe2, 4) followed by iodination in the presence of sodium methoxide in methanol affords (Z)-disubstituted alkenes (2) in good yields.Both procedures constitute a general one-pot synthesis of (Z)- disubstituted alkenes from an alkene and 1-alkyne.A simple synthesis of Muscalure (7), the sex pheromone of the housefly (Musca domestica), is achieved in good yields.An alternative general stereospecific synthesis of (Z)- and (E)-disubstituted alkenes based on alkenylboronic esters is also described.
